ENST00000342992.11:c.88328T>G
(TTN)
|
ENSP00000343764.6:p.Ile29443Arg
|
|
ENST00000342175.11:c.69413T>G
(TTN)
|
ENSP00000340554.6:p.Ile23138Arg
|
|
ENST00000359218.10:c.69212T>G
(TTN)
|
ENSP00000352154.5:p.Ile23071Arg
|
|
ENST00000342175.10:c.69413T>G
(TTN)
|
ENSP00000340554.6:p.Ile23138Arg
|
|
ENST00000342992.10:c.88328T>G
(TTN)
|
ENSP00000343764.6:p.Ile29443Arg
|
|
ENST00000359218.9:c.69212T>G
(TTN)
|
ENSP00000352154.5:p.Ile23071Arg
|
|
ENST00000460472.6:c.68837T>G
(TTN)
|
ENSP00000434586.1:p.Ile22946Arg
|
|
ENST00000589042.5:c.96032T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile32011Arg
|
|
ENST00000591111.5:c.91109T>G
(TTN)
|
ENSP00000465570.1:p.Ile30370Arg
|
|
ENST00000615779.4:c.91109T>G
(TTN)
|
ENSP00000483597.1:p.Ile30370Arg
|
|
NM_001256850.1:c.91109T>G
(TTN)
|
NP_001243779.1:p.Ile30370Arg
|
|
NM_001267550.2:c.96032T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile32011Arg
|
|
NM_003319.4:c.68837T>G
(TTN)
|
NP_003310.4:p.Ile22946Arg
|
|
NM_133378.4:c.88328T>G
(TTN)
|
NP_596869.4:p.Ile29443Arg
|
|
NM_133432.3:c.69212T>G
(TTN)
|
NP_597676.3:p.Ile23071Arg
|
|
NM_133437.4:c.69413T>G
(TTN)
|
NP_597681.4:p.Ile23138Arg
|
|
NR_038271.1:n.446+20476A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1751A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95129T>G
(TTN)
|
XP_011510031.1:p.Ile31710Arg
|
|
XM_011511730.1:c.69023T>G
(TTN)
|
XP_011510032.1:p.Ile23008Arg
|
|
XM_011511731.1:c.68882T>G
(TTN)
|
XP_011510033.1:p.Ile22961Arg
|
|
XM_017004819.1:c.94925T>G
(TTN)
|
XP_016860308.1:p.Ile31642Arg
|
|
XM_017004820.1:c.90323T>G
(TTN)
|
XP_016860309.1:p.Ile30108Arg
|
|
XM_017004821.1:c.90320T>G
(TTN)
|
XP_016860310.1:p.Ile30107Arg
|
|
XM_017004822.1:c.87362T>G
(TTN)
|
XP_016860311.1:p.Ile29121Arg
|
|
XM_017004823.1:c.68978T>G
(TTN)
|
XP_016860312.1:p.Ile22993Arg
|
|
XM_024453094.1:c.90473T>G
(TTN)
|
XP_024308862.1:p.Ile30158Arg
|
|
XM_024453095.1:c.90470T>G
(TTN)
|
XP_024308863.1:p.Ile30157Arg
|
|
XM_024453096.1:c.89903T>G
(TTN)
|
XP_024308864.1:p.Ile29968Arg
|
|
XM_024453097.1:c.87245T>G
(TTN)
|
XP_024308865.1:p.Ile29082Arg
|
|
XM_024453098.1:c.87164T>G
(TTN)
|
XP_024308866.1:p.Ile29055Arg
|
|
XM_024453099.1:c.68927T>G
(TTN)
|
XP_024308867.1:p.Ile22976Arg
|
|
XM_024453100.1:c.58781T>G
(TTN)
|
XP_024308868.1:p.Ile19594Arg
|
|